ArticleChemCatChem2025
Highly Enantioselective Synthesis of Halogenated Cyclopropanes via Enzyme Catalyzed Carbene Transfer.
Article in ChemCatChem, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
1 citing paper in PubMed.
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Authors and funding
7 authors.
Funding
Abstract
Halogenated cyclopropanes are highly desirable building blocks for both agrochemical and medicinal chemistry due to their unique structural features and ability to interact with biological targets through halogen bonds. However, methods for the highly diastreo- and enantioselective synthesis of these molecules are underdeveloped. Herein, we report the development of a new biocatalytic strategy to efficiently synthesize enantioenriched halogenated cyclopropanes through the enzymatic cyclopropanation of chloro- and bromo-substituted olefins in the presence of diazoacetonitrile using engineered myoglobin-based catalysts. This method tolerates a wide range of chloro- and bromo-containing olefins at both
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